2012
DOI: 10.1016/j.dyepig.2011.07.009
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New azodisperse dyes with thiazole, thiophene, pyridone and pyrazolone moiety for dyeing polyester fabrics

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Cited by 60 publications
(27 citation statements)
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“…IR spectra were recorded on Perkin-Elmer 1600 FTIR in KBr pellets. 1 H NMR spectra were taken on a Bruker Avance II 400 NMR MHz in DMSO as solvent and TMS as internal standard and elemental analysis of "Nitrogen" was carried on Carlo Erba 1108 instrument at SAIF Central Instrumentation Laboratory, Panjab University, Chandigarh. Absorption spectra of the dyes were recorded on a Shimadzu UV-1800 spectrophotometer in DMSO and water.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…IR spectra were recorded on Perkin-Elmer 1600 FTIR in KBr pellets. 1 H NMR spectra were taken on a Bruker Avance II 400 NMR MHz in DMSO as solvent and TMS as internal standard and elemental analysis of "Nitrogen" was carried on Carlo Erba 1108 instrument at SAIF Central Instrumentation Laboratory, Panjab University, Chandigarh. Absorption spectra of the dyes were recorded on a Shimadzu UV-1800 spectrophotometer in DMSO and water.…”
Section: Methodsmentioning
confidence: 99%
“…Disperse dyes are very important class of dyes due to their brilliancy, wide range of hue and excellent fastness properties 1,2 . They are used for dyeing hydrophobic fibres like nylon, polyester and acrylic fibres from an aqueous dispersion 3,4 .…”
Section: Introductionmentioning
confidence: 99%
“…Owing to their importance andu sefulness,anumber of methods for the preparation of pyrazoles have been developed. [10] Pyrazoles bearing an azo group (azopyrazoles) are also found as the core structurei nm any food colorings, [11] dyestuffs, [12] and bioactive molecules ( Figure 2). [13] They exhibited ab road spectrum of biologicalp roperties such as antibacterial, [14] antifungal [15] and HIV-1 inhibitory activities.…”
Section: Introductionmentioning
confidence: 99%
“…These dyes showed high ability as disperse dyes for dyeing polyester fabrics with acceptable fastness properties. 172 Diazotized aryl amines were coupled with 2-amino-4-substituted-thiazoles 3 to give 5-arylazo-2-aminothiazoles 120, which on reaction with different reagents, such as benzoyl chloride and acetic anhydride yielded the corresponding 2-(N-benzoylamino)-5-arylazothiazole derivatives 121 and 2-(N-acetylamino)-5-arylazothiazole 122. These mono azo dyes were applied to polyester as disperse dyes and their fastness properties were evaluated.…”
Section: Azo Coupling Reactionsmentioning
confidence: 99%